A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640944



Internal ID6681029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61133263..61139078hg38UCSC Ensembl
Innerchr17:61133280..61139062hg38UCSC Ensembl
Outerchr17:61133247..61139095hg38UCSC Ensembl
chr17:59210624..59216439hg19UCSC Ensembl
Innerchr17:59210641..59216423hg19UCSC Ensembl
Outerchr17:59210608..59216456hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg385816
hg195816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15716472
SamplesNA21119
Known GenesBCAS3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640944
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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